Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73058307-73058574 | Common:2; Rare:77 | ||||
chr14:73136302-73136541 | Common:4; Rare:76; Clinvar:4; Clinvar (benign):1 | ||||
chr14:73136880-73137150 | Common:1; Rare:55 | ||||
chr14:73457916-73457971 | Rare:14 | ||||
chr14:73458468-73458887 | Common:5; Rare:110 | ||||
chr14:73463567-73463830 | Common:1; Rare:46 | ||||
chr14:73787135-73787355 | Common:2; Rare:82 | ||||
chr14:73949982-73950310 | Common:7; Rare:128; Clinvar (benign):5 | ||||
chr14:74019259-74019352 | Rare:44 | ||||
chr14:74493267-74493770 | Common:4; Rare:160; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr14:74713075-74713203 | Rare:64 | ||||
chr14:75278340-75279168 | Common:4; Rare:212 | ||||
chr14:75279618-75279692 | Rare:10 | ||||
chr14:75279839-75279847 | Rare:1 | ||||
chr14:75280398-75280706 | Common:2; Rare:77 |